Evidence map›Paper›PMID 26136411›Full record

ArticleJournal of cachexia, sarcopenia and muscle2015

Influence of cancer cachexia on drug liver metabolism and renal elimination in rats.

Katja Cvan Trobec, Mojca Kerec Kos, Jurij Trontelj, Iztok Grabnar, Anika Tschirner, Sandra Palus, Stefan D Anker, Jochen Springer, Mitja Lainscak

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 29 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 2 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. PeerJ · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Inflammation-induced cholestasis in cancer cachexia.Journal of cachexia, sarcopenia and muscle · 2021
    Article
  14. Review
  15. Cancer Cachexia and Related Metabolic Dysfunction.International journal of molecular sciences · 2020
    Review
  16. Vancomycin Pharmacokinetics in Patients with Advanced Cancer Near End of Life.European journal of drug metabolism and pharmacokinetics · 2019
    Article
  17. Review
  18. Article
  19. Article
  20. Muscle wasting in heart failure : The role of nutrition.Wiener klinische Wochenschrift · 2016
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Katja Cvan TrobecFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Mojca Kerec KosFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Jurij TronteljFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Iztok GrabnarFaculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.
Anika TschirnerApplied Cachexia Research, Department of Cardiology, Charité Medical School, Campus Virchow-Klinikum, Berlin, Germany.
Sandra PalusDivision of Innovative Clinical Trials, Department of Cardiology & Pulmonology, University Medicine Göttingen (UMG), Göttingen, Germany.
Stefan D AnkerApplied Cachexia Research, Department of Cardiology, Charité Medical School, Campus Virchow-Klinikum, Berlin, Germany.
Jochen SpringerDivision of Innovative Clinical Trials, Department of Cardiology & Pulmonology, University Medicine Göttingen (UMG), Göttingen, Germany.
Mitja LainscakDepartment of Cardiology, General Hospital Celje, Celje, Slovenia.
University of Ljubljana · SICharité - Universitätsmedizin Berlin · DEUniversitätsmedizin Göttingen · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBody wasting and cachexia change body composition and organ function, with effects on drug pharmacokinetics. The aim of this study was to investigate how cancer and cancer cachexia modify liver metabolism and renal drug elimination in rats.

methodsNine male Wistar-Han rats received a single oral dose of midazolam and propranolol (markers of hepatic metabolism), and 10 rats received single intravenous dose of iohexol, a marker of glomerular filtration rate. After drug delivery, multiple dried blood samples were obtained within 2 h post-dose to evaluate drug pharmacokinetic profiles. After baseline sampling (D0), rats were injected with tumour cells. Drug application and blood sampling were repeated when rats developed tumours (Day 5-D5), and when rats were severely cachectic (Day 10-D10). Clearance (CL) and volume of distribution (Vd) of drugs were assessed with non-linear mixed effects modelling. Weight and body composition were measured on D0 and D10 and were related to pharmacokinetic parameters.

resultsAll three drugs showed non-significant trend towards increased CL and Vd on D5. On D10, midazolam and propranolol CL and midazolam Vd significantly decreased from baseline (-80.5%, -79.8%, and -72.0%, respectively, P < 0.05 for all). Iohexol CL decreased by 29.8% from baseline value on D10, which was related to body weight loss (Pearson's r = 0.837, P = 0.019).

conclusionsHepatic metabolism and renal drug elimination are significantly reduced in cachexia, which could increase risk of dose-related adverse events.

Indexed as

CachexiaCancerDrug metabolismLiver metabolismPharmacokineticRenal function

Identifiers

PMID26136411
PMCPMC4435096
OpenAlexW1912151765

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.